|
|
| ID |
SNP51.300 |
| OMIM_ID |
tggcttcatccctcaactgatgctttccta
|
| Disease |
DIGEORGE SYNDROME |
| Gene |
TBX1(T-box1)
|
| SNP_ID |
rs5746832
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
SNP:
single nucleotide polymorphism
|
| Alleles |
A/G
|
| Orientation |
T-box1 |
| Chr-Number |
chromosome 22 |
| SNP
type |
fwd/T |
| Length |
R |
| 5'
Near Seq 30 bp |
801 |
| 3'
Near Seq 30 bp |
cacaccctgtggccgttgtccccatcgtcc |
| Fasta
Sequence |
>gnl|dbSNP|rs5746832|allelePos=401|totalLen=801|taxid=9606|snpclass=1|alleles='A/G'|mol=Genomic|build=127
AGGATGAGGC CAAATGACTC GATTTCTCTA CACCCCACAT TTTACAGGTT TCAGAGCCCA
AGTCAGGAGG TCAAGTGTGC ATGCAAGAGG TGGCAGGGGA CAGATGTGCT GCTGTTCCCA
GGCCACCTGC ACAGCTGGAT GGTGGAAGCA GTTCACTTAA AGGCCATGag ttactcggga
ggctgaggca ggaggatcac ttgagcctat tagttggagg ctgcagtaag ctatgatcat
gccactgcac tccagcctgg gtgacagagt gagaccccca ctgtccctgg tctcttaaaa
gaaaaaacaa acaaacaaac caaaaaaCAA AACAGCTTAT GAGCACCTCC TACTAATTTC
CTCAGCTTAG CACACCCTGT GGCCGTTGTC CCCATCGTCC
R
TGGCTTCATC CCTCAACTGA TGCTTTCCTA TGTGGACTTC CCGGCCAGTG CTGTGGGACC
TCCCCTGTAG GGCTGGCCAG CCTCATGGGC TGGGCTACCC GTCCCACTCA GCAGTGGCTG
CCTGGCCTCC CCTCTGTCCC TCCTGCCCAG CTCCTAATGG GCCTCCCATA AAAGCTGATG
CGTGGGAGCC AAGCCACAGC TCGCTGACCT GGGGAAGCTG ACAGAGTGAC AGAGGGTCTC
AAGGACTCTC CACCCACAAG GCGGGAATGG GGATGCTGGC AAATCTGGTA TGAAGGTTGA
GACCCCGAGG AGAGGCAGGC CTGGGGGACC GTGCAGCAGC TGTGCCCACC TAGGACCACA
GGGCTGGTGG GGCTGGCAGC TTGGTAGAGG GCAGGTGCAC
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